Last updated on July 2017

A Study of MEDI9197 in Subjects With Solid Tumors or CTCL and in Combination With Durvalumab and/or Palliative Radiation in Subjects With Solid Tumors


Brief description of study

To evaluate MEDI9197 when administered by intratumoral injection to subjects with solid tumors or CTCL, and in combination with durvalumab and/or palliative radiation in subjects with solid tumors.

Detailed Study Description

This is a multicenter, unblinded study to evaluate the TLR 7/8 agonist MEDI9197 delivered by IT injection to subjects with solid tumors or CTCL, and in combination with durvalumab and/or palliative radiation in subjects with solid tumors. The study uses a 3 + 3 dose escalation design to evaluate a range of doses.

Clinical Study Identifier: NCT02556463

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AstraZeneca Clinical Study Information Center

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San Francisco, CA United States
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AstraZeneca Clinical Study Information Center

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Aurora, CO United States
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AstraZeneca Clinical Study Information Center

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Tampa, FL United States
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AstraZeneca Clinical Study Information Center

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Minneapolis, MN United States
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AstraZeneca Clinical Study Information Center

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New York, NY United States
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AstraZeneca Clinical Study Information Center

Research Site
Chapel Hill, NC United States
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AstraZeneca Clinical Study Information Center

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Houston, TX United States
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